Impact of medium cut-off membranes on S100A12 and soluble receptor for advanced glycation end products

被引:3
|
作者
Korucu, Berfu [1 ]
Yeter, Hasan [1 ]
Gonen, Sevim [2 ]
Derici, Mehmet Kursat [3 ]
Ronco, Claudio [4 ]
Derici, Ulver [1 ]
机构
[1] Gazi Univ, Fac Med, Dept Nephrol, Ankara, Turkey
[2] Gazi Univ, Fac Med, HLA Tissue Typing Lab, Ankara, Turkey
[3] Kirikkale Univ, Fac Med, Dept Pharmacol, Ankara, Turkey
[4] San Bortolo Hosp, Int Renal Res Inst, Dept Nephrol Dialysis & Kidney Transplant, Vicenza, Italy
关键词
UREMIC TOXINS; HEMODIALYSIS; ATHEROSCLEROSIS; RAGE; CALCIFICATION; MORTALITY; DIALYZERS; HEART; SRAGE; RISK;
D O I
10.1111/sdi.13107
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction Of the most remarkable molecules associated with atherosclerosis and the cardiovascular outcome are S100A12 (10,379.5 Da) and soluble receptor for advanced glycation end products (sRAGE-42,803 Da) in the hemodialysis (HD) population. We designed a study investigating the effects of the medium cut-off (MCO) dialyzers focusing on S100A12 and sRAGE in HD patients compared with low-flux and high-flux dialyzers. Methods This single-site, prospective, observational study comprises age and sex-matched HD groups (low-flux, high-flux, and MCO). Blood samples were drawn at baseline (predialysis and postdialysis) and the sixth month (predialysis). Results Groups had similar demographic features and laboratory parameters. Baseline S100A12 levels of the groups were similar [34.3 (+/- 66.5), 30.9 (+/- 42.7), and 40.6 (+/- 29.6); p = 0.13]. Compared to their baseline, the sixth-month S100A12 levels were constant in low-flux and high-flux group and significantly lower in MCO group (p = 0.16, p = 0.33, and p = 0.004). Baseline sRAGE levels of the groups were similar at baseline [2.8 (+/- 0.8), 2.7 (+/- 0.6), and 2.6 (+/- 0.7); p = 0.65], and the sixth-month [2.9 (+/- 0.5), 2.4 (+/- 0.7), and 2.4 (+/- 0.8); p = 0.24]. sRAGE levels remained constant in all groups [p = 0.84, p = 0.13, and p = 0.39]. S100A12/sRAGE ratio at baseline and sixth month was constant in low-flux [22.3 (+/- 63.7) and 18.1 (+/- 24.8); p = 0.17] and high-flux groups [11.9 (+/- 15.3) and 13.1 (+/- 5.8); p = 0.26], the ratio decreased significantly in MCO group [16.5 (+/- 11.6) to 7.8 (+/- 5.5); p = 0.03]. Conclusion Our study suggests that prolonged use of MCO dialyzers is associated with better S100A12 and sRAGE levels. Long-term studies with larger samples are needed to understand the effects of a better S100A12-sRAGE profile provided by MCO dialyzers on HD patients' cardiovascular outcomes.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 50 条
  • [21] Soluble Receptor for Advanced Glycation End Products: a new biomarker in diagnosis of Diabetic Nephropathy
    Issa, Hesham A.
    Elshaer, Osama S.
    Awadallah, Ahmed M.
    El-Adl, Tawfik
    LIFE SCIENCE JOURNAL-ACTA ZHENGZHOU UNIVERSITY OVERSEAS EDITION, 2012, 9 (04): : 1623 - 1629
  • [22] Serum levels of soluble receptor for advanced glycation end products (sRAGE) in Takayasu's arteritis
    Mahajan, Nitin
    Dhawan, Veena
    Malik, Sonal
    Jain, Sanjay
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 145 (03) : 589 - 591
  • [23] Receptor for Advanced Glycation End Products and Soluble Receptor for Advanced Glycation End Products: A Balancing Act in Chronic Obstructive Pulmonary Disease?
    Sukkar, Maria B.
    Postma, Dirkje S.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 188 (08) : 893 - 894
  • [24] Plasma advanced glycation end products and soluble receptor for advanced glycation end products as indicators of sterol content in human carotid atherosclerotic plaques
    Pinto, Raphael S.
    Ferreira, Guilherme S.
    Silvestre, Gina Camillo R.
    Santana, Monique de Fatima M.
    Nunes, Valeria S.
    Ledesma, Lucas
    Pinto, Paula R.
    de Assis, Sayonara Ivana S.
    Machado, Ubiratan F.
    da Silva, Erasmo S.
    Passarelli, Marisa
    DIABETES & VASCULAR DISEASE RESEARCH, 2022, 19 (01)
  • [25] Soluble receptor for advanced glycation end products in late onset neonatal infection
    Zolakova, B.
    Zolak, V
    Hatok, J.
    Matasova, K.
    Nosal, S.
    Zibolen, M.
    BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY, 2016, 117 (01): : 15 - 18
  • [26] Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis
    Manichaikul, Ani
    Sun, Li
    Borczuk, Alain C.
    Onengut-Gumuscu, Suna
    Farber, Emily A.
    Mathai, Susan K.
    Zhang, Weiming
    Raghu, Ganesh
    Kaufman, Joel D.
    Hinckley-Stukovsky, Karen D.
    Kawut, Steven M.
    Jelic, Sanja
    Liu, Wen
    Fingerlin, Tasha E.
    Schwartz, David A.
    Sell, Jessica L.
    Rich, Stephen S.
    Barr, R. Graham
    Lederer, David J.
    ANNALS OF THE AMERICAN THORACIC SOCIETY, 2017, 14 (05) : 628 - 635
  • [27] Statins stimulate the production of a soluble form of the receptor for advanced glycation end products
    Quade-Lyssy, Patricia
    Kanarek, Anna Maria
    Baiersdoerfer, Markus
    Postina, Rolf
    Kojro, Elzbieta
    JOURNAL OF LIPID RESEARCH, 2013, 54 (11) : 3052 - 3061
  • [28] Independent determinants of soluble form of receptor for advanced glycation end products in elderly hypertensive patients
    Nakamura, Kazuo
    Adachi, Hisashi
    Matsui, Takanori
    Kurita, Yayoi
    Takeuchi, Masayoshi
    Yamagishi, Sho-ichi
    METABOLISM-CLINICAL AND EXPERIMENTAL, 2009, 58 (03): : 421 - 425
  • [29] Decreased levels of soluble receptor for advanced glycation end products in patients with primary Sjogren's syndrome
    Stewart, Carol
    Cha, Seunghee
    Caudle, Robert M.
    Berg, Kathleen
    Katz, Joseph
    RHEUMATOLOGY INTERNATIONAL, 2008, 28 (08) : 771 - 776
  • [30] Relationship Between Levels of Advanced Glycation End Products and Their Soluble Receptor and Adverse Outcomes in Adults With Type 2 Diabetes
    Thomas, Merlin C.
    Woodward, Mark
    Neal, Bruce
    Li, Qiang
    Pickering, Raelene
    Marre, Michel
    Williams, Bryan
    Perkovic, Vlado
    Cooper, Mark E.
    Zoungas, Sophia
    Chalmers, John
    Hillis, Graham S.
    DIABETES CARE, 2015, 38 (10) : 1891 - 1897